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5 days ago
This is a position for highly motivated individuals who are passionate about regulatory affairs and quality system implementation to ensure that medical products, vaccines and other health technologies in the market meet internationally recognized standards of quality, safety, and efficacy.
**Responsibilities**:
- Establish and execute regulatory strategies to meet the requirements of various stakeholders
- Develop documentations and deliver compliance plans and quality planning strategy
- Proactively identify new opportunities and deliver innovative solutions to address customers’ needs
- Perform additional ad-hoc duties as assigned from time to time
**Requirements**:
- Diploma/ Degree in Biomedical/ Science/ Engineering or other relevant fields
- Relevant experience in pharmaceutical or medical devices regulatory affairs and knowledge of quality assurance is an advantage
- Responsible, work independently, detail oriented
- Able to manage and prioritize multiple projects and tasks to meet deadlines
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